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Familial Hypomagnesemia With Secondary Hypocalcemia: A Case Report
Familial hypomagnesemia with secondary hypocalcemia is a rare genetic disorder of magnesium metabolism that presents with refractory seizures during infancy. It is caused by loss-of-function mutations in the gene encoding transient receptor potential cation channel member 6 (TRPM6). Herein we report...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702611/ https://www.ncbi.nlm.nih.gov/pubmed/34963857 http://dx.doi.org/10.7759/cureus.19847 |